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Journal of Neuromuscular Diseases|May 13, 2025
A prospective observational study assessing the functional disease progression of LGMDR4, betasarcoglycan-related limb girdle muscular dystrophyMegan A Iammarino, Natalie F Reash, Kiana Shannon, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 14, 2011
Chondroitinase ABC combined with neurotrophin NT-3 secretion and NR2D expression promotes axonal plasticity and functional recovery in rats with lateral hemisection of the spinal cordGuillermo García-Alías, Hayk A Petrosyan, Lisa Schnell, et al.Plos Neglected Tropical Diseases|July 11, 2014
Hematogenously disseminated Orientia tsutsugamushi-infected murine model of scrub typhus [corrected]Thomas R Shelite, Tais B Saito, Nicole L Mendell, et al.Muscle & Nerve|January 1, 1987
Clinical investigation in Duchenne dystrophy. VI. Double-blind controlled trial of nifedipineR T Moxley, M H Brooke, G M Fenichel, et al.American Journal of Human Genetics|June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.Nature Genetics|June 1, 1993
Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination eventsB Weiffenbach, J Dubois, D Storvick, et al.Clinical Chemistry|January 1, 1995
A molecular protocol for diagnosing myotonic dystrophyM Guida, R S Marger, A C Papp, et al.Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|August 6, 2011
Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2IXiomara Q Rosales, Sean J Moser, Tam Tran, et al.Journal of Human Genetics|June 24, 2011
Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spotCharlotte A Brown, Juergen Scharner, Kevin Felice, et al.Journal of Translational Medicine|September 26, 2007
A translational approach for limb vascular delivery of the micro-dystrophin gene without high volume or high pressure for treatment of Duchenne muscular dystrophyLouise R Rodino-Klapac, Paul M L Janssen, Chrystal L Montgomery, et al.Pageof 89